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Evaluation of Clinical Features and Surgical Outcomes of the Too Long Anterior Process in Children

Evaluation of Clinical Features and Surgical Outcomes of the Too Long Anterior Process in Children: a Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04894942
Enrollment
11
Registered
2021-05-20
Start date
2021-07-31
Completion date
2021-12-31
Last updated
2021-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Calcaneonavicular Coalition

Brief summary

Calcaneonavicular coalition represents approximately 1% of the population between 8 and 12 years. They are manifested by repeated ankle sprains or by pain. - The diagnosis is radiological on an X-ray of the foot in oblique-3/4 incidence as well as magnetic resonance imaging. Treatment is second-line surgery after failure of orthopedic treatment. This surgery is either by direct approach or by arthroscopy, by performing a bone resection to recreate sufficient space in the joint in question. The patients in this study will only be operated on openly.

Interventions

OTHERAmerican Orthopaedic Foot and Ankle Society Score (AOFASS)

calculation of the score AOFASS before and after the surgery

Sponsors

University Hospital, Limoges
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
8 Years to 16 Years

Inclusion criteria

* Child \<16 years * Child with calcaneonavicular coalition * Magnetic resonance imaging diagnosis * Patient already treated orthopedically in the initial treatment of the coalition

Exclusion criteria

* Child \>=16 years

Design outcomes

Primary

MeasureTime frameDescription
Comparison of scores before surgery and after surgery at 1 month, for all the operated patients1 monthCalculation of the American Orthopaedic Foot and Ankle Society Score. This is an instrument for measuring the outcome of treatment in patients who sustained a complex ankle or hindfoot injury. It combines a clinician-reported and a patient-reported part. The maximal score is 100 points, indicating no symptoms or impairments.
Comparison of scores before surgery and after surgery at 3 months for all the operated patients3 monthsCalculation of the American Orthopaedic Foot and Ankle Society Score. This is an instrument for measuring the outcome of treatment in patients who sustained a complex ankle or hindfoot injury. It combines a clinician-reported and a patient-reported part. The maximal score is 100 points, indicating no symptoms or impairments.
Comparison of scores before surgery and after surgery at 1 12 months for all the operated patients12 monthsCalculation of the American Orthopaedic Foot and Ankle Society Score. This is an instrument for measuring the outcome of treatment in patients who sustained a complex ankle or hindfoot injury. It combines a clinician-reported and a patient-reported part. The maximal score is 100 points, indicating no symptoms or impairments.

Countries

France

Contacts

Primary ContactQuentin Ballouhey, MD
quentin.ballouhey@unilim.fr0555049027
Backup ContactQuentin Ballouhey, MD
quentin.ballouhey@unilim.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026